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Exposure to Organochlorine Pollutants and Impact on Development in the Peripubertal Age in Guadeloupe

Exposure to Organochlorine Pollutants and Impact on Development in the Peripubertal Age in Guadeloupe

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06653660
Acronym
TIMOUNPUBERTY
Enrollment
650
Registered
2024-10-22
Start date
2022-12-19
Completion date
2026-12-19
Last updated
2025-11-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postnatal Exposure, Prenatal Exposure

Keywords

Prenatal Exposure, Postnatal Exposure, Chlordecone, Persistent Organic Pollutants, Endocrine disruptors, Puberty, Development, Guadeloupe, French West Indies

Brief summary

In the context of environmental pollution of the French West Indies by chlordecone and questions about health consequences, monitoring at the peripubertal age of children born alive in the TIMOUN cohort is justified in several respects: - existence of an already established mother-child cohort whose live-born children will reach peripubertal ages during the period 2020-2022; - opportunity to verify hypotheses put forward on the basis of toxicological data acquired in laboratory animals and the hormonal characteristics of chlordecone (endocrine disruptor); - strong societal demand for such research to be carried out because of concerns about the sensitivity of children and adolescents to the effects of environmental xenobiotics, in particular on sexual development and the age of puberty; - recommendation of the Scientific Council Chlordecone Inserm - InVS; specific action of the National Plan Chlordecone IV.

Detailed description

The French West Indies are permanently polluted by chlordecone. It is an organochlorine insecticide used from 1973 to 1993 in Guadeloupe and Martinique to control banana root borers. Its physico-chemical properties give it great stability and are at the origin of its persistence in the environment. Soil, flora and wildlife pollution from chlordecone in the Caribbean was first documented shortly after its introduction in 1973. However, it was not until 1999 that this pollution was extended to waters intended for human consumption and to various local, vegetable and animal, land and aquatic foodstuffs. The population is also affected, as confirmed by impregnation studies, with exposure nowadays occurring mainly through the consumption of contaminated food. The contamination of the French West Indies populations by this insecticide raises many questions about its possible health consequences. In order to assess the effects of chlordecone exposure on child development in Guadeloupian children, a longitudinal and prospective study, the Timoun mother-child cohort, was initiated. Between 2004 and 2007, women in the second trimester of pregnancy who planned to give birth in the public hospitals of Grande-Terre and Basse-Terre (accounting for 70% of all deliveries in Guadeloupe) were invited to participate in the study. Children born to these included women have been enrolled to several follow-ups during the last years (3, 7, 18 months and 7 years of age).

Interventions

OTHERClinical examination

For the aim of the present study, we will follow-up children born alive in the TIMOUN cohort at peripubertal age. Questionnaires will be administered to parents on the child's health and lifestyle. Stature-weight anthropometric and cardio-dynamic measurements of the child will be obtained. Scores on three cognitive tests will be obtained. Furthermore, steroid hormones and chlordecone in the child's peripheral blood will be determined.

Sponsors

Institut National de la Santé Et de la Recherche Médicale, France
CollaboratorOTHER_GOV
Centre Hospitalier Universitaire de la Guadeloupe
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
16 Years to 22 Years
Healthy volunteers
No

Inclusion criteria

* Be born to a mother whose pregnancy was included in the Timoun cohort (2004 - 2007) and whose parents agreed to be contacted later. * Residing in Guadeloupe at the peripubertal age * Affiliation to a social security scheme * Agreement to participate in the study and informed consent signed by the minor * Study participation agreement and informed consent signed by the parents

Exclusion criteria

* Refusal to participate in the research

Design outcomes

Primary

MeasureTime frameDescription
Scores from cognitive development tests estimating verbal comprehension verbal comprehension, perceptual reasoning and working memoryAt the start of the study (inclusion visit): Cognitive tests (25 min for the 3 Wechsler Intelligence Scale for Children V subscales). The Wechsler Intelligence Scale for Children-V is the most scientifically valid intelligence test for children and adolescents. It can be used to determine a child's or teenager's intelligence quotient (IQ), to obtain their complete cognitive profile and the level of the 5 main components of cognitive intelligence

Secondary

MeasureTime frameDescription
Age at onset of pubertal development (onset of accelerated growth acceleration of growth rate, modeled on growth curves)At the start of the study (inclusion visit).Collect of the age at which children and adolescents begin to develop adult physical characteristics, such as breasts or pubic hair, and become able to procreate.

Other

MeasureTime frameDescription
Age at established puberty (period for girls, molting for boys)At the start of the study (inclusion visit) or through study completion, an average of two years, for girls who had their period and boys molted.Collect of the age at which girls had their period and boys molted
Plasma concentrations of steroid hormonesAt the start of the study (inclusion visit).Blood collection for hormonal and organochlorine pollutants dosage.
Blood pressureAt the start of the study (inclusion visit).Seated resting blood pressure will be measured using an automatic tensiometer an automatic blood pressure monitor, with two measurements separated by 15 to 30 minutes.
heart rateAt the start of the study (inclusion visit).heart ratewill be measured using an automatic tensiometer an automatic blood pressure monitor, with two measurements separated by 15 to 30 minutes.

Countries

Guadeloupe

Contacts

Primary ContactValérie HAMONY-SOTER
valerie.soter@chu-guadeloupe.fr+590 590 93 46 77
Backup ContactEunice NUBRET
eunice.nubret@chu-guadeloupe.fr+590 590 93 46 86

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026